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dc.contributor.authorFava, Rafaela Marono-
dc.contributor.authorFerragut Cardoso, Ana Paula-
dc.contributor.authorRocha, Mitscheli Sanches da-
dc.contributor.authorNascimento e Pontes, Merielen Garcia-
dc.contributor.authorViana de Camargo, Joao Lauro-
dc.contributor.authorCotrim Sartor de Oliveira, Maria Luiza-
dc.date.accessioned2015-10-21T13:09:27Z-
dc.date.accessioned2016-10-25T20:59:29Z-
dc.date.available2015-10-21T13:09:27Z-
dc.date.available2016-10-25T20:59:29Z-
dc.date.issued2015-07-03-
dc.identifierhttp://www.sciencedirect.com/science/article/pii/S0300483X15000773-
dc.identifier.citationToxicology. Clare: Elsevier Ireland Ltd, v. 333, p. 100-106, 2015.-
dc.identifier.issn0300-483X-
dc.identifier.urihttp://hdl.handle.net/11449/128385-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/128385-
dc.description.abstractDiuron [3-(3,4-dichlorophenyl)-1,1-dimethylurea] is a substituted urea herbicide carcinogenic to the rat urinary bladder at high dietary levels. The suggested non-genotoxic mode of action (MOA) of diuron encompasses cytotoxicity and necrosis followed by regenerative hyperplasia. Prenecrotic swollen cells as observed under scanning electron microscopy (SEM) have been reported as early morphological alterations, putatively related to diuron cytotoxicity. However, these changes were not observed in a previous SEM study conducted in this laboratory. This study evaluated whether these early alterations are actually due to diuron cytotoxicity or artifacts related to different processing methods used for SEM analysis. Male Wistar rats were fed ad libitum with basal diet, 7.1% sodium saccharin (NaS) or 2.500 ppm diuron for seven days or 15 weeks. The urinary bladders were processed for histological and labeling indices examinations and for SEM using two different processing methods. The incidence of simple hyperplasia after 15 weeks of exposure to diuron or to NaS was significantly increased. By SEM, the incidences and severity of lesions were significantly increased in the diuron group independently of exposure time. The different SEM processing methods used allowed for visualization of swollen superficial cells after seven days of diuron exposure. Probably the absence these cells in a previous study was due to the use very few animals. Our results support the hypothesis that the swollen cell is an early key event due to diuron-induced cytotoxicity and is the result of a degenerative process involved in the non-genotoxic carcinogenic mode of action of high doses of diuron.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)-
dc.description.sponsorshipCenter for the Evaluation of the Environmental Impact on Human Health (TOXICAM), Department of Pathology, Sao Paulo State University (UNESP) Medical School, Botucatu, SP, Brazil-
dc.format.extent100-106-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectDiuron[3-(3,4-dichlorophenyl)-1,1-dimethylurea]en
dc.subjectCarcinogenesisen
dc.subjectEarly changeen
dc.subjectRat urinary bladderen
dc.subjectScanning electron microscopyen
dc.subjectSwollen cellsen
dc.titleEvaluation of early changes induced by diuron in the rat urinary bladder using different processing methods for scanning electron microscopyen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionPlanitox-
dc.description.affiliationSão Paulo State University (UNESP) - Center for the Evaluation of the Environmental Impact on Human Health (TOXICAM), Department of Pathology, Botucatu Medical School, Botucatu, São Paulo 18618-970, Brazil-
dc.description.affiliationPlanitox, Campinas, 13024-230 SP, Brazil-
dc.description.affiliationUnespSão Paulo State University (UNESP) - Center for the Evaluation of the Environmental Impact on Human Health (TOXICAM), Department of Pathology, Botucatu Medical School, Botucatu, São Paulo 18618-970, Brazil-
dc.description.sponsorshipIdFAPESP: 2012/11210-3-
dc.identifier.doihttp://dx.doi.org/10.1016/j.tox.2015.04.006-
dc.identifier.wosWOS:000357228200010-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofToxicology-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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